Details

Autor(en) / Beteiligte

• Zwisler, Ann-Dorthe
• Rossau, Henriette Knold
• Nakano, Anne
• Foghmar, Sussie
• Eichhorst, Regina
• Prescott, Eva
• Cerqueira, Charlotte
• Soja, Anne Merete Boas
• Gislason, Gunnar H
• Larsen, Mogens Lytken
• Andersen, Ulla Overgaard
• Gustafsson, Ida
• Thomsen, Kristian K
• Boye Hansen, Lene
• Hammer, Signe
• Viggers, Lone
• Christensen, Bo
• Kvist, Birgitte
• Lindström Egholm, Cecilie
• May, Ole

Titel

The Danish Cardiac Rehabilitation Database

Ist Teil von

• Clinical epidemiology, 2016-01, Vol.8, p.451-456

Ort / Verlag

New Zealand: Dove Medical Press Limited

Erscheinungsjahr

2016

Quelle

EZB Electronic Journals Library

Beschreibungen/Notizen

• The Danish Cardiac Rehabilitation Database (DHRD) aims to improve the quality of cardiac rehabilitation (CR) to the benefit of patients with coronary heart disease (CHD). Hospitalized patients with CHD with stenosis on coronary angiography treated with percutaneous coronary intervention, coronary artery bypass grafting, or medication alone. Reporting is mandatory for all hospitals in Denmark delivering CR. The database was initially implemented in 2013 and was fully running from August 14, 2015, thus comprising data at a patient level from the latter date onward. Patient-level data are registered by clinicians at the time of entry to CR directly into an online system with simultaneous linkage to other central patient registers. Follow-up data are entered after 6 months. The main variables collected are related to key outcome and performance indicators of CR: referral and adherence, lifestyle, patient-related outcome measures, risk factor control, and medication. Program-level online data are collected every third year. Based on administrative data, approximately 14,000 patients with CHD are hospitalized at 35 hospitals annually, with 75% receiving one or more outpatient rehabilitation services by 2015. The database has not yet been running for a full year, which explains the use of approximations. The DHRD is an online, national quality improvement database on CR, aimed at patients with CHD. Mandatory registration of data at both patient level as well as program level is done on the database. DHRD aims to systematically monitor the quality of CR over time, in order to improve the quality of CR throughout Denmark to benefit patients.